| Protocol No. | UW24141 OSU-23199 |
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|---|---|---|---|
| Principal Investigator | Sahasrabudhe, Kieran | ||
| Phase | I | ||
| Age Group | Adult | ||
| ClinicalTrials.Gov | NCT06222580 (Click to jump to clinicaltrials.gov) | ||
| Management Group(s) | Early Phase | ||
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Title
Description
Objective
Treatment
This phase I trial tests the safety, side effects, and best dose of SNDX-5613 and gilteritinib for treating patients with acute myeloid leukemia that has come back after a period of improvement (relapsed) or that does not respond to treatment (refractory) and has a mutation in the FLT3 gene along with either a mutation in the NMP1 gene or a type of mutation called a rearrangement in the MLL gene. SNDX-5613 is in a class of medications called menin inhibitors. It works by blocking the action of mutated MLL and NMP1 proteins that signal cancer cells to multiply. Gilteritinib is in a class of medications called tyrosine kinase inhibitors. It works by blocking the action of mutated FLT3 proteins that signal cancer cells to multiply. Giving SNDX-5613 with gilteritinib may be safe, tolerable and/or effective in treating patients with relapsed/refractory FLT3 mutated acute myeloid leukemia.
Key Eligibility
For full study eligibility, see this study's ClinicalTrials.gov record.
Applicable Disease Sites
Participating Institutions
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